For researchers

Is your paper here?

2,681 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

37 matches for Asselbergs FW, showing the first 20.

Seventy-five genetic loci influencing the human red blood cell
Nature · 2012 · PMID 23222517
12 pages+
rs901683 rs10849023 rs3892630 rs4953318 rs243070 rs10207392
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs10843164 rs10182181 rs1412239 rs1421085 rs538656 rs1514177
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs3739707 rs6137287 rs9993613 rs3020418 rs3767627 rs7692995
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs2820443 rs12955983 rs6737082 rs2821248 rs10840060 rs4727804
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs9891146 rs13447324 rs5758651 rs34149579 rs12236219 rs284860
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
Nature communications · 2018 · PMID 30046033 · open access
12 pages+
rs13018106 rs12678719 rs11465506 rs397637 rs4430933 rs6599250
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Nature communications · 2018 · PMID 30194396 · open access
12 pages+
rs551980034 rs479404 rs540409605 rs35569312 rs148143917 rs754058883
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
European journal of human genetics : EJHG · 2019 · PMID 30679814 · open access
12 pages+
rs6489973 rs3757868 rs432256 rs6911599 rs9385199 rs2074518
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Communications biology · 2020 · PMID 32327693 · open access
12 pages+
rs62063786 rs480299 rs12373123 rs34453673 rs155779 rs28462342
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs149165710 rs145441283 rs187207161 rs767105335 rs77357563 rs2306899
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs111589301 rs12992267 rs141350130 rs7410608 rs186398347 rs3135688
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6058896 rs649523 rs6552828 rs3806325 rs7162940 rs7219047
Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity
Science advances · 2023 · PMID 37126556 · open access
12 pages+
rs2696421 rs4835730 rs12452627 rs567642046 rs7774130 rs4835729
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs7311187 rs113520491 rs17122659 rs4678604 rs6505204 rs6919654
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs67377357 rs149780392 rs3794752 rs62233286 rs7095308 rs73048654
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Nature genetics · 2021 · PMID 33495596 · open access
10 pages
rs2668674 rs8039472 rs4820654 rs66761782 rs4385202 rs10927875
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Nature communications · 2018 · PMID 30410027 · open access
9 pages
rs381949 rs10054105 rs200476 rs72878024 rs8853 rs1638703
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
8 pages
rs12012576 rs6527977 rs139120857 rs5942972 rs7063103 rs62603531

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Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.